Euroopan unioni - suomi - EMA (European Medicines Agency)

almirall s.a - tildrakizumab - psoriasis - immunosuppressantit, interleukiinin estäjät, - ilumetri on tarkoitettu hoitoon aikuisilla, joilla on kohtalainen tai vaikea läiskäpsoriaasi, jotka ovat ehdokkaita systeeminen hoito.

Euroopan unioni - suomi - EMA (European Medicines Agency)

shionogi b.v. - naldemedine tosilate - ummetus - lääkkeet ummetus, perifeerinen opioidi-reseptorin antagonistit - rizmoic on tarkoitettu hoitoon opioidien aiheuttama ummetus (oic) aikuisilla potilailla, joille on aiemmin hoidettu laksatiivinen.

Euroopan unioni - suomi - EMA (European Medicines Agency)

kyowa kirin holdings b.v. - mogamulizumab - sezary syndrome; mycosis fungoides - antineoplastiset aineet - poteligeo on tarkoitettu aikuisille potilaille, joilla on t-solulymfooman (mf) tai sézary oireyhtymä (ss), jotka ovat saaneet vähintään yksi aikaisempi systeeminen hoito.

Suomi - suomi - Fimea (Suomen lääkevirasto)

drossapharm arzneimittel handelsgesellschaft gmbh - etofenamate - lääkelaastari - 70 mg - etofenamaatti

Euroopan unioni - suomi - EMA (European Medicines Agency)

albireo - odevixibat - cholestasis, intrahepatic - bile- ja maksanhoito - bylvay is indicated for the treatment of progressive familial intrahepatic cholestasis (pfic) in patients aged 6 months or older (see sections 4. 4 ja 5.

Euroopan unioni - suomi - EMA (European Medicines Agency)

celltrion healthcare hungary kft. - regdanvimab - covid-19 virus infection - immunoseerumit ja immunoglobuliinit, - regdanvimab is indicated for the treatment of adults with coronavirus disease 2019 (covid-19) who do not require supplemental oxygen and who are at increased risk of progressing to severe covid-19.

Euroopan unioni - suomi - EMA (European Medicines Agency)

accord healthcare s.l.u. - plerixafor - multiple myeloma; hematopoietic stem cell transplantation - immunostimulantit, - adult patientsplerixafor accord is indicated in combination with granulocyte-colony stimulating factor (g-csf) to enhance mobilisation of haematopoietic stem cells to the peripheral blood for collection and subsequent autologous transplantation in adult patients with lymphoma or multiple myeloma whose cells mobilise poorly (see section 4. paediatric patients (1 to less than 18 years)plerixafor accord is indicated in combination with g-csf to enhance mobilisation of haematopoietic stem cells to the peripheral blood for collection and subsequent autologous transplantation in children with lymphoma or solid malignant tumours, either:- pre-emptively, when circulating stem cell count on the predicted day of collection after adequate mobilization with g-csf (with or without chemotherapy) is expected to be insufficient with regards to desired hematopoietic stem cells yield, or- who previously failed to collect sufficient haematopoietic stem cells (see section 4.

Suomi - suomi - Fimea (Suomen lääkevirasto)

seacross pharma (europe) limited - plerixafor - injektioneste, liuos - 20 mg/ml - pleriksafori

Suomi - suomi - Fimea (Suomen lääkevirasto)

galderma nordic ab - lymecycline - kapseli, kova - 150 mg - lymesykliini

Suomi - suomi - Fimea (Suomen lääkevirasto)

galderma nordic ab - lymecycline - kapseli, kova - 300 mg - lymesykliini